» Articles » PMID: 20047871

On 'various Contrivances': Pollination, Phylogeny and Flower Form in the Solanaceae

Overview
Specialty Biology
Date 2010 Jan 6
PMID 20047871
Citations 29
Authors
Affiliations
Soon will be listed here.
Abstract

Members of the euasterid angiosperm family Solanaceae have been characterized as remarkably diverse in terms of flower morphology and pollinator type. In order to test the relative contribution of phylogeny to the pattern of distribution of floral characters related to pollination, flower form and pollinators have been mapped onto a molecular phylogeny of the family. Bilateral flower symmetry (zygomorphy) is prevalent in the basal grades of the family, and more derived clades have flowers that are largely radially symmetric, with some parallel evolution of floral bilateralism. Pollinator types ('syndromes') are extremely homoplastic in the family, but members of subfamily Solanoideae are exceptional in being largely bee pollinated. Pollinator relationships in those genera where they have been investigated more fully are not as specific as flower morphology and the classical pollinator syndrome models might suggest, and more detailed studies in some particularly variable genera, such as Iochroma and Nicotiana, are key to understanding the role of pollinators in floral evolution and adaptive radiation in the family. More studies of pollinators in the field are a priority.

Citing Articles

Evolution and development of complex floral displays.

Khojayori F, Ponraj U, Buch K, Zhao Y, Herrera-Ubaldo H, Glover B Development. 2024; 151(21).

PMID: 39498660 PMC: 11574353. DOI: 10.1242/dev.203027.


Lack of pollinators selects for increased selfing, restricted gene flow and resource allocation in the rare Mediterranean sage Salvia brachyodon.

Surina B, Balant M, Glasnovic P, Gogala A, Fiser Z, Satovic Z Sci Rep. 2024; 14(1):5017.

PMID: 38424151 PMC: 10904396. DOI: 10.1038/s41598-024-55344-7.


Genome-wide identification and evolutionary view of ALOG gene family in Solanaceae.

Turchetto C, Silverio A, Waschburger E, Lacerda M, Quintana I, Turchetto-Zolet A Genet Mol Biol. 2023; 46(3 Suppl 1):e20230142.

PMID: 38048778 PMC: 10695626. DOI: 10.1590/1415-4757-GMB-2023-0142.


Global distribution and evolutionary transitions of floral symmetry in angiosperms.

Wang Y, Luo A, Lyu T, Dimitrov D, Liu Y, Li Y Sci Adv. 2023; 9(43):eadg2555.

PMID: 37878700 PMC: 10599613. DOI: 10.1126/sciadv.adg2555.


Honesty, reliability, and information content of floral signals.

van der Kooi C, Reuvers L, Spaethe J iScience. 2023; 26(7):107093.

PMID: 37426347 PMC: 10329176. DOI: 10.1016/j.isci.2023.107093.


References
1.
Perez F, Arroyo M, Medel R . Phylogenetic analysis of floral integration in Schizanthus (Solanaceae): does pollination truly integrate corolla traits?. J Evol Biol. 2007; 20(5):1730-8. DOI: 10.1111/j.1420-9101.2007.01393.x. View

2.
Palma G, Quezada-Euan J, Melendez-Ramirez V, Irigoyen J, Valdovinos-Nunez G, Rejon M . Comparative efficiency of Nannotrigona perilampoides, Bombus impatiens (Hymenoptera: Apoidea), and mechanical vibration on fruit production of enclosed habanero pepper. J Econ Entomol. 2008; 101(1):132-8. DOI: 10.1603/0022-0493(2008)101[132:ceonpb]2.0.co;2. View

3.
Stone J, Sasuclark M, Blomberg C . Variation in the self-incompatibility response within and among populations of the tropical shrub Witheringia solanacea (Solanaceae). Am J Bot. 2011; 93(4):592-8. DOI: 10.3732/ajb.93.4.592. View

4.
. On the Various Contrivances by Which British and Foreign Orchids Are Fertilized by Insects; and on the Good Effects of Intercrossing. Br Foreign Med Chir Rev. 2018; 30(60):312-318. PMC: 5180317. View

5.
Perez F, Arroyo M, Medel R, Hershkovitz M . Ancestral reconstruction of flower morphology and pollination systems in Schizanthus (Solanaceae). Am J Bot. 2011; 93(7):1029-38. DOI: 10.3732/ajb.93.7.1029. View